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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T36879L | H-Leu-Leu-OMe . HBr | H-Leu-Leu-OMe . HBr (16689-14-8 Free base) | Others |
H-Leu-Leu-OMe . HBr is a dipeptide condensation product of L-leucine methyl ester generated by human monocytes or polymorphonuclear leukocytes. H-Leu-Leu-OMe . HBr induces endolysosomal pathway stress and selectively eli... | |||
TP1212 | N-Boc-Phe-Leu-Phe-Leu-Phe | Boc-FLFLF | Others |
N-Boc-Phe-Leu-Phe-Leu-Phe (Boc-FLFLF) (Boc-FLFLF) is a formyl peptide receptor 1 (FPR1) antagonist, which increases pain effects and inhibits antinociceptive activity of annexin. Boc-Phe-Leu-Phe-Leu-Phe is used extensive... | |||
TMA2613 | Cyclo(Pro-Leu) | Cyclo-L-leu-L-pro,Cyclo-L-prolyl-L-leucine,Cyclo(leucyloprolyl) | Others |
Cyclo(Pro-Leu) (Cyclo-L-prolyl-L-leucine) is a marine-derived natural product with brine shrimp lethality. | |||
TN6444 | Cyclo(Tyr-Leu) | Antifungal | |
Cyclo(Tyr-Leu) is a cyclic dipeptide from Portulaca oleracea Linn with cytotoxicity, antifungal, and anticoagulant activities. | |||
T7739 | L-Leucyl-L-Leucine methyl ester hydrochloride | Leu-Leu-ome hydrochloride | Others , Endogenous Metabolite |
L-Leucyl-L-Leucine methyl ester hydrochloride (Leu-Leu-ome hydrochloride) is a lysosomal condensation product that cytotoxic towards natural killer cells and CD4+ and CD8+ T lymphocytes. | |||
T36352 | Suc-Leu-Tyr-AMC | ||
Suc-Leu-Tyr-AMC is a fluorescent substrate for calpain I and II and papain (another cysteine protease) that is used for measuring the chymotrypsin-like peptidase activity of the 20S proteasome (excitation max: 360 nm; em... | |||
TP1164 | N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA | For-Nle-Leu-Phe-Nle-Tyr-Lys-OH (TFA) | Others |
N-Formyl-Nle-Leu-Phe-Nle-Tyr-Lys TFA (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH (TFA)) (For-Nle-Leu-Phe-Nle-Tyr-Lys-OH TFA) is a formyl peptide receptor (FPR) agonist[1].Potent chemoattractant for human neutrophils.Radioiodinated m... | |||
T22752L | (D-Ser2)-Leu-Enkephalin-Thr | Opioid Receptor | |
(D-Ser2)-Leu-Enkephalin-Thr is a delta selective agent of opioid receptor and shows analgesic effects. | |||
TP1168 | N-Formyl-Met-Leu-Phe-Lys | fMLFK | Others |
N-Formyl-Met-Leu-Phe-Lys (fMLFK) (fMLFK) is a peptide, acts as a potent and selective agonist of FPR1, with EC50s of 3.5 nM, 6.7 μM and 0.88 μM for FPR1, FPR2 and FPR2-D2817.32G, respectively.Chemotactic peptide (fMLFK) ... | |||
T8557 | N-terminally acetylated Leu-enkephalin | Opioid Receptor | |
Leu-enkephalin, an endogenous peptide consisting of five amino acids, functions as an agonist at opioid receptors. The N-terminally acetylated form of this compound is known as N-terminally acetylated Leu-enkephalin. | |||
TP1399 | Fmoc-N-Me-Leu-OH | Others | |
Fmoc-N-Me-Leu-OH is available for the peptide-coupling reaction. | |||
T7091 | N-Formyl-Met-Leu-Phe | fMLP,N-Formyl-MLF | TNF |
N-Formyl-Met-Leu-Phe (N-Formyl-MLF) (fMLF) is a synthetic peptide that acts as an agonist at formyl peptide receptors (FPR; Ki = 0.8 pM). | |||
T80665 | Leu-Val | L-leucyl-L-valine | Parasite , Antifungal |
Leu-Val (L-leucyl-L-valine) is a novel potent dipeptide with antibacterial and antimalarial activity. | |||
TP2507 | Leu-Tyr-Asp-Lys | ||
Leu-Tyr-Asp-Lys is a tetrapeptide compound that can be used to study metabolism-related diseases. | |||
TP2305 | PGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val | Others | |
pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val is a peptides | |||
T2154 | MG-132 | Z-LLL-al,Z-Leu-Leu-Leu-CHO | Apoptosis , Proteasome , Autophagy |
MG-132 (Z-Leu-Leu-Leu-al) is a 26S proteasome inhibitor (IC50=100 nM) that is cell-permeable and reversible. MG-132 acts as an autophagy activator and also induces apoptosis. | |||
T125115 | Cyclo(L-Leu-L-Pro) | Antifungal | |
Cyclo(L-Leu-L-Pro) is a compound from Pseudomonas sesquiterpenes BC42 that exhibits antifungal activity, inhibits fungal pathogens, and inhibits the proliferation of Aspergillus flavus.Cyclo(L-Leu-L-Pro) inhibits conidia... | |||
T4086 | Glycyl-L-leucine | Gly-Leu | Others |
Glycyl-L-leucine (Gly-Leu) is a substrate for the assay of glycyl-L-leucine dipeptidase. | |||
T40768 | {Boc}-Phe-Leu-Phe-Leu-Phe | ||
{Boc}-Phe-Leu-Phe-Leu-Phe ({Boc}-FLFLF) is a selective antagonist of the formyl peptide receptor (FPR) family, effectively inhibiting receptor activity in response to formyl peptides. | |||
TN6681 | Cyclo(Leu-Leu) | ||
Cyclo(Leu-Leu) is an efficient supramolecular catalyst. |